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Recent Advances in Visible-Light-Induced Organic Phosphine- Promoted Deoxygenative Functionalization Reactions

  • Juan Tang ,
  • Jiayu Hu ,
  • Zhiqiang Zhu ,
  • Shouzhi Pu
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  • a Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013
    b Key Laboratory for Green Chemistry of Jiangxi Province, Jiangxi Normal University, Nanchang 330022
    c Jiangxi Province Key Laboratory of Synthetic Chemistry, East China University of Technology, Nanchang 330013

Received date: 2023-05-11

  Revised date: 2023-07-06

  Online published: 2023-08-30

Supported by

National Natural Science Foundation of China(21864013); National Natural Science Foundation of China(22263005); Natural Science Foundation of Jiangxi Province(20212BCJL23057); Natural Science Foundation of Jiangxi Province(20224ACB203006); Natural Science Foundation of Jiangxi Province(20232BAB203001); Postdoctoral Foundation of Jiangxi Province(2019KY40)

Abstract

Organic phosphine-promoted organic synthesis reactions have developed rapidly in recent years. Triphenylphos- phine and their derivatives are the most important class of organic phosphine compounds, which can not only serve as ligands in organic synthesis reactions, but also serve as deoxygenative promoters in a large number of reactions. In recent years, visible-light-induced deoxygenative coupling reactions have aroused considerable attention. This type of reaction uses organic phosphines to promote single electron transfer to form P—O intermediates with oxygen-containing organic molecules under visible-light, followed by deoxidation to obtain highly active free radical species, and then deoxygenative coupling to afford the desired products. Herein, the recent research progress in photoredox-induced organic phosphine-promoted deoxygenative functionalization reactions is summarized.

Cite this article

Juan Tang , Jiayu Hu , Zhiqiang Zhu , Shouzhi Pu . Recent Advances in Visible-Light-Induced Organic Phosphine- Promoted Deoxygenative Functionalization Reactions[J]. Chinese Journal of Organic Chemistry, 2023 , 43(12) : 4036 -4056 . DOI: 10.6023/cjoc202305012

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